通过独特型操作诱导小鼠IV型胶原非胶原结构域(NC1)抗体。

Human antibodies and hybridomas Pub Date : 1995-01-01
Y Shoenfeld, B Gilburd, M Hojnik, M Damianovich, S Hacham, Y Kopolovic, P Polak-Charcon, I Goldberg, A Afek, L Hun-Chi
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引用次数: 0

摘要

Goodpasture综合征(GPS)的特征性致病性自身抗体指向基底膜IV型胶原的非胶原结构域(NC1)。为了研究抗nc1抗体免疫是否会导致类似GPS的病理,我们用小鼠抗nc1单克隆抗体或来自GPS患者的血清IgG片段皮内免疫BALB/c小鼠。用正常小鼠或人IgG免疫小鼠和未免疫小鼠作为对照。注射抗nc1抗体小鼠血清中检测到IgG同型的抗nc1抗体,而对照组血清中未检测到IgG同型的抗nc1抗体。循环抗nc1抗体的存在与一些小鼠红细胞尿症或蛋白尿和肾脏病理改变相吻合。对照组小鼠未见病理改变。结果表明,特异性独特型操作可诱导抗nc1抗体和类似人类GPS的病理变化。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Induction of Goodpasture antibodies to noncollagenous domain (NC1) of type IV collagen in mice by idiotypic manipulation.

The characteristic pathogenic autoantibodies in Goodpasture's syndrome (GPS) are directed to the noncollagenous domain (NC1) of basement membrane type IV collagen. To examine whether immunization with anti-NC1 antibodies could lead to GPS-like pathology, naive BALB/c mice were immunized intradermally with a mouse IgG anti-NC1 monoclonal antibody or IgG serum fraction derived from patients with GPS. Mice immunized with normal mouse or human IgG and nonimmunized mice served as controls. Anti-NC1 antibodies of IgG isotype were detected in the sera of mice injected with anti-NC1 antibodies, but not in the sera of control mice. The presence of circulating anti-NC1 antibodies coincided in some of the mice erythrocyturia or proteinuria and pathological changes in the kidneys. No pathologic alterations were seen in the control mice. The results show that specific idiotypic manipulation can induce anti-NC1 antibodies and pathological changes resembling human GPS.

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